# K061952: Cardiovascular Array Coils, Models Cac-63-16, Cac-63-32, Cac-123-32 and Cac-127-16

- Pathway: 510(k) (Special)
- Applicant: Invivo
- Decided: Jul 28, 2006 after 18 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K212239: XENOVIEW 3.0T Chest Coil (2022), 2 descendants of its own
- K231647: XENOVIEW 3.0T Chest Coil (2023), 1 descendant of its own
- K243316: XENOVIEW 3.0T Chest Coil (2024), 0 descendants of its own
- K183186: Head Coil – 12, Head Coil – 32, Carotid Coil – 8, Temporomandibular Joint Coil – 4, Infant Coil – 24, Cardiac Coil – 24, Foot & Ankle Coil - 24 (2019), 0 descendants of its own
- K120290: Toshiba 1.5T Cardiac Coil (2012), 0 descendants of its own

## Indications for use
To be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the cardiovascular, pulmonary, renal, and abdominal systems that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K061952
Methodology: https://510kreport.com/methodology